Anti-properdin antibodies, and methods for making and using same

a technology of properdin and antibodies, applied in the field of antibodies, can solve the problems of cellular damage through insertion into cell membranes, inappropriate activation of complement, and potential harm to the host, and achieve the effects of reducing the number of antibodies

Inactive Publication Date: 2006-05-04
AMGEN FREMONT INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

While complement activation provides a valuable first line of defense against pathogens, inappropriate activation of complement poses potential harm to the host.
These anaphylatoxins initiate a cellular inflammatory response that is beneficial in the case of a pathogenic infection, but is potentially detrimental when inappropriately generated.
For example, MAC causes cellular damage through its insertion into cell membranes.
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Method used

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  • Anti-properdin antibodies, and methods for making and using same
  • Anti-properdin antibodies, and methods for making and using same
  • Anti-properdin antibodies, and methods for making and using same

Examples

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Effect test

example 1

Preparation and Characterization of Anti-Properdin Monoclonal Antibodies

Summary

[0165] The aim of this study was to identify fully human monoclonal antibodies (MoAbs) that bind to human properdin with high affinity and block the complement alternative pathway. Since it is important that these MoAbs do not themselves trigger inflammation via activation of complement or Fcy receptors, IgG2 and IgG4 XenoMouse strains were targeted for immunization. Human properdin was used as the immunogen and several IgG2 and IgG4 XenoMouse animals received either footpad or tail-vein immunizations. Fusions with splenocytes from both IgG2 and IgG4 animals were performed, and IgG2 hybridoma supernatant samples were determined to bind to human properdin. These samples were evaluated for their ability to neutralize properdin function. The results reveal that several of the fully human anti-properdin MoAbs block properdin function.

Materials and Methods

Generation of Hybridomas

[0166] Xenomouse animal...

example 2

Anti-Properdin Nonoclonal Antibodies Inhibit C3c and sC5b-9 Generation in 8% Human Serum

Materials and Methods

Human C3c and sMAC ELISA Assay

[0186] Sigma S. typhosa LPS L6386 (25 mg / sample) was used. LPS (3 mg) was dissolved in 1 ml of carbonate buffer, and diluted to 20 μg / ml in carbonate buffer (1:150 dilution). LPS stock solution was made fresh before use. Wells were coated overnight at 4° C. with 50 μl / well of 20 μg / ml LPS in 50 mM carbonate buffer pH 9.5 (1 μg LPS / well).

[0187] Carbonate buffer was made by dissolving 0.265g of Na2CO3 in 50 ml sterile H2O for 50 mM stock solution. AP Buffer (13 mM EGTA, 13 mM MgCl2 in Gelatin Veronal Buffer (Sigma-Aldrich, Catalog number: G6514) pH 7.3) was made. As a negative control, 13 mM EDTA in Gelatin Veronal Buffer was used. Human serum (QED BioScience, Inc.) was prepared by diluting human serum to 16% with AP buffer, or with EDTA-Gelatin Veronal Buffer. Antibody samples were diluted to a concentration of 180 μg / ml in 2 mg / ml BSA-PBS a...

example 3

The Effects of Anti-Properdin Monoclonal Antibodies on Inhibition of Complement Activation in a Tubing Loop Model of Cardiopulmonary Bypass

Experimental Design

[0192] In this experiment, tubing loops were filled with 1.5 ml of diluted blood from a healthy volunteer. The tubing loops were rotated vertically in a water bath at 37° C. for 2 hours to allow for complement activation to occur. Blood samples from the tubing loops were transferred into polypropylene tubes that were pre-loaded with EDTA for determining complement activation. The addition of EDTA prevents further complement activation that would otherwise occur during sample processing. Blood samples were centrifuged to separate plasma and aliquoted for analysis.

Materials / Reagents

[0193] Blood (25 ml) was collected in a 50-ml polypropylene tube containing 125 μl of porcine heparin. Blood was diluted 1:1 with plasmalyte-148 (Baxter Healthcare Corporation) for a final heparin concentration of 2.5 units per ml of diluted bloo...

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Abstract

The present invention is related to antibodies directed to the antigen properdin and uses of such antibodies. In particular, in accordance with the present invention, there are provided fully human monoclonal antibodies directed to the antigen properdin. Nucleotide sequences encoding, and polypeptides comprising, heavy and light chain immunoglobulin molecules, particularly sequences corresponding to contiguous heavy and light chain sequences spanning the framework regions and/or complementarity determining regions (CDR's), specifically from FR1 through FR4 or CDR1 through CDR3, are provided. Hybridomas or other cell lines expressing such immunoglobulin molecules and monoclonal antibodies are also provided.

Description

FIELD OF THE INVENTION [0001] The present invention is in the field of antibodies, and in particular, antibodies specific for properdin. BACKGROUND OF THE INVENTION [0002] The complement system provides an early acting mechanism to initiate and amplify the inflammatory response to microbial infection and other acute insults. While complement activation provides a valuable first line of defense against pathogens, inappropriate activation of complement poses potential harm to the host. For instance, the complement system has been implicated in contributing to the pathogenesis of several acute and chronic conditions, including post-cardiopulmonary bypass inflammation, myocardial infarction, stroke, acute respiratory distress syndrome (ARDS), septic shock, transplant rejection, burn injury, multiple sclerosis, myasthenia gravis, and rheumatoid arthritis. It is important to note that while complement may not be the sole cause of pathogenesis in these conditions, complement activation app...

Claims

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Application Information

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IPC IPC(8): A61K39/395C07K16/46C07K16/44
CPCC07K16/18C07K2316/96C07K2317/21C07K2317/54C07K2317/76A61P11/00A61P13/12A61P17/02A61P19/02A61P21/04A61P25/28A61P29/00A61P31/04A61P37/06A61P43/00A61P9/00A61P9/02A61P9/10
Inventor GAZIT-BORNSTEIN, GADISENALDI, GIORGIOYANG, XIAO-DONGKEYT, BRUCEZAPATA, GERARDO
Owner AMGEN FREMONT INC
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